Please visit "Birdshot Uveitis Society":http://www.birdshot.org.uk. This is the site we are launching specifically for people with Birdshot Chorioretinopathy. We are called Birdshot Uveitis Society and are based in the UK. Please note all birdshot sufferers are welcome although you will see that the information is partly geared towards the health service in the UK. Wherever you live, we'd like to be able to keep in touch with you and tell you about any new developments in treatment of birdshot which may develop. We hope the registration will be a simple process and if you get stuck send us an email and we can guide you through it. NB The Registration Link is at the bottom of the page on the righthand side! For those who want to increase text size control plus works well in many browsers. We are affiliated to the Uveitis Information Group which is a UK charity which provides patient information and support for people diagnosed with uveitis. We are a voluntary organisation ie no one gets paid! If anyone needs particular information about Birdshot Chorioretinopathy you are welcome to email us and we can see if we can help. We hope that our new site will be especially useful for people who are newly diagnosed. www.birdshot.org.uk Annie

Hi Annie: Thanks for launching this site. I have seen your posts on the US site with Dagmar as well. I wish these sites had been available when I was diagnosed 4 1/2 years ago. These forums are great for education and support. Thanks again. Shelley

Shelley, I fully agree with you. They are both doing a great job! I was diagnosed around the time the UK site was being set up so I was lucky. Dagmar's enthusiasm is great. One day I will tell her! All the best Adrian